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FDA 510(k)

ROSENBERG SKIN GRAFTING KNIVES

K-Number: K842702 · 1984-08-02

ApplicantDowns Surgical , Ltd.
Decision Date1984-08-02
Product CodeGFD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ROSENBERG SKIN GRAFTING KNIVES is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K842702. The device is classified under product code GFD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROSENBERG SKIN GRAFTING KNIVES?

ROSENBERG SKIN GRAFTING KNIVES is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K842702.

When did ROSENBERG SKIN GRAFTING KNIVES receive FDA 510(k) clearance?

ROSENBERG SKIN GRAFTING KNIVES received FDA 510(k) clearance on 1984-08-02, under 510(k) number K842702.

Who is the listed applicant for ROSENBERG SKIN GRAFTING KNIVES?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROSENBERG SKIN GRAFTING KNIVES?

The FDA product code for ROSENBERG SKIN GRAFTING KNIVES is GFD.

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Other records listing Downs Surgical , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K903750ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-EK903747ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-UK903749ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-UK903748ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-VK900609SHEPPERD STRAIGHT AND CURVED NEEDLESK900616SHEPPERD CUTTING FORCEPS

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Related Devices (Code: GFD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K965256DMS-1000C DERMOABRADERMattioli Engineering, SrlK962371DERMTOME BLADEDsp WorldwideK945594DECA DERMATOME (MICROMOTOR SYSTEM)Depuy Intl., Ltd.K951085PADGETT AIR DERMATOME, MODEL APadgett Instruments, Inc.K940208AESCULAP ACCU-DERMATOMEAesculap, Inc.K862669ACTIVATED PARTIAL THROMBOPLASTIN TIME TESTU. S. Diagnostics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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